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Awaiting hospital appt
Hi I've had a letter through the post saying I have a small AN and now awaiting specialist appointment at Salford. I've had symptoms of tinnitus my referral to ENT was my ask not GPs and I was surprised when the ENT consultant offered me an MRI to put my mind at ease. I was expecting it to come back
Hi I've had a letter through the post saying I have a small AN and now awaiting specialist appointment at Salford. I've had symptoms of tinnitus my referral to ENT was my ask not GPs and I was surprised when the ENT consultant offered me an MRI to put my mind at ease. I was expecting it to come back
Ranikhan
in
Acoustic Neuroma Support
6 months ago
narrow angles
Hi, first post on this forum, new to all of this. On a recent trip to the opticians, my wife (56) was referred to our local eye clinic with narrow drainage angles. Her ocular pressure is ok and there are no other abnormalities. The referral was quick and she had an appointment at the clinic within
Hi, first post on this forum, new to all of this. On a recent trip to the opticians, my wife (56) was referred to our local eye clinic with narrow drainage angles. Her ocular pressure is ok and there are no other abnormalities. The referral was quick and she had an appointment at the clinic within
AAJJTt
in
Glaucoma UK
7 months ago
Permanently damaged vision due to dry eyes?
I've had Limited Scleroderma for about 12 years. A year ago, I noticed that the vision in my left eye had become blurred. 3 opticians and 4 opthalmologists later (because I never see the same person twice, and every one starts at the beginning - what a ludicrous system), we have finally reached the
I've had Limited Scleroderma for about 12 years. A year ago, I noticed that the vision in my left eye had become blurred. 3 opticians and 4 opthalmologists later (because I never see the same person twice, and every one starts at the beginning - what a ludicrous system), we have finally reached the
Lausanjuk
in
Scleroderma & Raynaud's UK (SRUK)
7 months ago
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Recurrant water infections
Hello everyone I keep getting water infections but there is no bacteria in my urine now my doctor is sending me for ultra sound on my kidneys iam so worried.
Hello everyone I keep getting water infections but there is no bacteria in my urine now my doctor is sending me for ultra sound on my kidneys iam so worried.
Tojack
in
Women's Health
2 months ago
Probiotics
Hi I've had ibs c for so so long. Over the years I've learnt what does and doesn't suit me with my diet. I'm now mainly ok in comparison but also as I've got older I get bouts of diarrhea which I know are from eating foods that don't agree with me. I had a fair amount of cream cake over Christmas I'm
Hi I've had ibs c for so so long. Over the years I've learnt what does and doesn't suit me with my diet. I'm now mainly ok in comparison but also as I've got older I get bouts of diarrhea which I know are from eating foods that don't agree with me. I had a fair amount of cream cake over Christmas I'm
Gizmo6
in
IBS Network
3 months ago
Bladder pain
Started b12 injections (sc) approx 6 weeks ago and have been experiencing bladder irritation and pain. Is this related to b12 injections? Otherwise feeling positive about the treatment. I've been ill for many years so not expecting to improve overnight. Thank you.
Started b12 injections (sc) approx 6 weeks ago and have been experiencing bladder irritation and pain. Is this related to b12 injections? Otherwise feeling positive about the treatment. I've been ill for many years so not expecting to improve overnight. Thank you.
Shelley1234567
in
Pernicious Anaemia Society
7 months ago
piles and constipation
hi I’m 24 weeks and 3 days pregnant and have got piles all I’m doing is drinking fluid sticking to fruit veg and hi fibre foods I also have 4 other children I’m using paracetamol and laxative s along with cream I’ve had them 6 days now it really really hurts any advice welcome thanks for reading xx
hi I’m 24 weeks and 3 days pregnant and have got piles all I’m doing is drinking fluid sticking to fruit veg and hi fibre foods I also have 4 other children I’m using paracetamol and laxative s along with cream I’ve had them 6 days now it really really hurts any advice welcome thanks for reading xx
Loulou123886
in
Pregnancy and Parenting Support
3 months ago
Gastroperesis + IBS C- thoughts
Hello ! My name is Jess and I have been dealing with Gastroperesis for over 25 years. I am SOOOO tired of it! I constantly get a distended bloated stomach, some from gas and some from the slow digestion and not be able to go. I also have IBS-C ( constipation) so this makes matters worse. I take
Hello ! My name is Jess and I have been dealing with Gastroperesis for over 25 years. I am SOOOO tired of it! I constantly get a distended bloated stomach, some from gas and some from the slow digestion and not be able to go. I also have IBS-C ( constipation) so this makes matters worse. I take
jr188
in
IBS Network
3 months ago
GCA diagnostic dilemma
Thank you everyone who has helped so far. Last night I had a message from Rheumy saying I should go to the hospital for an emergency biopsy, with the headache and unusual severe temporal pain being the driver. He said that U/S was so ‘operator sensitive’ as to be unreliable in this ‘locality’. The
Thank you everyone who has helped so far. Last night I had a message from Rheumy saying I should go to the hospital for an emergency biopsy, with the headache and unusual severe temporal pain being the driver. He said that U/S was so ‘operator sensitive’ as to be unreliable in this ‘locality’. The
Predderman2020
in
PMRGCAuk
7 months ago
Colon inflammation on CT scan
Thank you for your replies to my previous post. I really appreciate people sharing their experiences with me. I ended up back in the emergency department on Thursday this week as my pain has increased so much. After more bloods I was taken for a CT scan with contrast. Spoke with doctors then following
Thank you for your replies to my previous post. I really appreciate people sharing their experiences with me. I ended up back in the emergency department on Thursday this week as my pain has increased so much. After more bloods I was taken for a CT scan with contrast. Spoke with doctors then following
Lastboyscout6
in
IBS Network
3 months ago
Polychromasia in peripheral smear?
I'm 23 M Jak2 negative, bmb inconclusive, done in 2018 Recent peripheral smear shows anisocytosis and polychromasia. Is this worrisome feature? Am i landing up in something serious?
I'm 23 M Jak2 negative, bmb inconclusive, done in 2018 Recent peripheral smear shows anisocytosis and polychromasia. Is this worrisome feature? Am i landing up in something serious?
Xuzy
in
MPN Voice
7 months ago
hi anyone had a gallblader removed
hi i had my gallblader removed in late september and since then iv feel like my bladder is full seem like i need to go urgently when i need to uranite and im getting up 3 or 4 times in the night . i dont know if it my gallbladder op thats causing it or its something to go with my bladder i had sitched
hi i had my gallblader removed in late september and since then iv feel like my bladder is full seem like i need to go urgently when i need to uranite and im getting up 3 or 4 times in the night . i dont know if it my gallbladder op thats causing it or its something to go with my bladder i had sitched
Mrshappyme
in
Pelvic Pain Support Network
7 months ago
2nd short term Ginkgo trial underway
The 1st was around 10 days ago. 1 tablet taken evening of purchase, and 3 over the following day. The day after that T was not around in the afternoon for a few hours. I thought I had been cured (!) but did come back around 6pm. 3 tablets also taken over that day. The following day T was around and it
The 1st was around 10 days ago. 1 tablet taken evening of purchase, and 3 over the following day. The day after that T was not around in the afternoon for a few hours. I thought I had been cured (!) but did come back around 6pm. 3 tablets also taken over that day. The following day T was around and it
Ray200
in
Tinnitus UK
7 months ago
Ophthalmologist Visit
I just wanted to report on the exam by the ophthalmologist today. He said everything looks good. Optic nerve looks fine. He agreed (with all of you!) that my visual disturbances are caused by the steroids. He recommended I talk to my optometrist about prism lenses that will help to correct the double
I just wanted to report on the exam by the ophthalmologist today. He said everything looks good. Optic nerve looks fine. He agreed (with all of you!) that my visual disturbances are caused by the steroids. He recommended I talk to my optometrist about prism lenses that will help to correct the double
Lenore58
in
PMRGCAuk
7 months ago
Affect of tummy upsets on anti-coagulants,
I was wondering what effect it has on the absorption of anti-coagulants, should something cause you to have diarrhoea - how long does it take after ingestion does it take something like an Eliquis tablet to become effective ?
I was wondering what effect it has on the absorption of anti-coagulants, should something cause you to have diarrhoea - how long does it take after ingestion does it take something like an Eliquis tablet to become effective ?
pusillanimous
in
AF Association
7 months ago
Regular care
I was diagnosed with AF around four years ago now, by a cardiologist in a major teaching hospital. I was put on anticoagulants and referred back to my GP. The local surgery check my meds yearly and I have an annual blood test, but that’s it. I am wondering whether I should ask to be referred back to
I was diagnosed with AF around four years ago now, by a cardiologist in a major teaching hospital. I was put on anticoagulants and referred back to my GP. The local surgery check my meds yearly and I have an annual blood test, but that’s it. I am wondering whether I should ask to be referred back to
AstroFish
in
Atrial Fibrillation Support
7 months ago
Aortitis
I was diagnosed with non cranial Giant Cell Arteritis in September last year. So far I haven't managed to find anyone else with this condition because most people have the temporal version with the headaches.Mine is Aortitis which apparently is rare. I'd love to share experiences with someone else
I was diagnosed with non cranial Giant Cell Arteritis in September last year. So far I haven't managed to find anyone else with this condition because most people have the temporal version with the headaches.Mine is Aortitis which apparently is rare. I'd love to share experiences with someone else
Dance62
in
PMRGCAuk
2 months ago
Blood pressure medication
Can anyone advise the best blood pressure medication that doesn't make breathlessness and dry cough worse. Also doesn't make your ankles swell.Really appreciate any recommendations as I am not sure the gp has the time to go into the different types. Have tried ramipri and amlodipine. Thank you
Can anyone advise the best blood pressure medication that doesn't make breathlessness and dry cough worse. Also doesn't make your ankles swell.Really appreciate any recommendations as I am not sure the gp has the time to go into the different types. Have tried ramipri and amlodipine. Thank you
Teralea
in
Lung Conditions Community Forum
7 months ago
GCA Eyesight Anxiety
Hello, I am feeling quite anxious now, because my long-distance sight seems worse today. I am definitely seeing double (at a distance) and cannot focus (distance only.) Up close is clear. (I do have myopia, and have never had any problem with close work, unlike most people my age, which is 65.) I was
Hello, I am feeling quite anxious now, because my long-distance sight seems worse today. I am definitely seeing double (at a distance) and cannot focus (distance only.) Up close is clear. (I do have myopia, and have never had any problem with close work, unlike most people my age, which is 65.) I was
Lenore58
in
PMRGCAuk
7 months ago
PMR and brachial neuritis
It looks like I have developed a fairly rare condition called Parsonage-Turner syndrome (PTS), also called brachial neuritis. It started with terrible pain in the shoulder, so initially I thought it would appear in the other shoulder and be the beginning of a PMR relapse. But it is taking a different
It looks like I have developed a fairly rare condition called Parsonage-Turner syndrome (PTS), also called brachial neuritis. It started with terrible pain in the shoulder, so initially I thought it would appear in the other shoulder and be the beginning of a PMR relapse. But it is taking a different
dmart7
in
PMRGCAuk
2 months ago
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